A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041417



Internal ID19130636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45525733..45592613hg38UCSC Ensembl
Innerchr10:46021181..46088061hg19UCSC Ensembl
Innerchr10:45341187..45408067hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3866881
hg1966881
hg1866881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv730n100
Supporting Variantsnssv3707815, nssv3519576
Samples
Known GenesMARCH8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041417
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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